647824-46-2 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
1-(TERT-BUTYL)-3,5-DIMETHYL-1H-PYRAZOLE is used as a key building block in the synthesis of various pharmaceuticals and agrochemicals, leveraging its unique structure and reactivity to create compounds with desired therapeutic or pesticidal properties.
Used in Dye and Pigment Production:
In the dye and pigment industry, 1-(TERT-BUTYL)-3,5-DIMETHYL-1H-PYRAZOLE is utilized for the production of dyes and pigments, contributing to the development of colorants with specific characteristics for various applications.
Used in Specialty Chemicals:
1-(TERT-BUTYL)-3,5-DIMETHYL-1H-PYRAZOLE is employed in the production of specialty chemicals, where its unique chemical properties are harnessed to create compounds with specific functionalities for use in various industrial applications.
Used in Research and Development:
1-(TERT-BUTYL)-3,5-DIMETHYL-1H-PYRAZOLE is used as a subject of research for its potential biological activities, such as anti-inflammatory and antitumor properties, with the aim of discovering new therapeutic agents or applications in medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 647824-46-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,7,8,2 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 647824-46:
(8*6)+(7*4)+(6*7)+(5*8)+(4*2)+(3*4)+(2*4)+(1*6)=192
192 % 10 = 2
So 647824-46-2 is a valid CAS Registry Number.
647824-46-2Relevant academic research and scientific papers
Scope and limitations in the regioselective synthesis of 1,3,5-trisubstituted pyrazoles from β-amino enones and hydrazine derivatives. 13C-chemical shift prediction rules for 1,3,5-trisubstituted pyrazoles
Alberola, Angel,Calvo Bleye, Luis,Gonza?lez-Ortega, Alfonso,Sa?daba, M.Luisa,San?udo, M.Carme
, p. 331 - 352 (2007/10/03)
β-amino enones react with hydrazine derivatives to give regioselectively 1,3,5-trisubstituted pyrazoles. The synthetic method only presents limitations when the β-substituent of the enone and the hydrazine substituent are bulky or possess an electron withdrawing character. Comparison of the 13C-NMR spectra of the seventy pyrazoles allowed us to estimate a 13C-chemical shift prediction rule for 1,3,5-trisubstituted pyrazoles, with deviations of less than ± 1 ppm.
